JP2012231165A - Deposition of silicon germanium on silicon-on-insulator structures and bulk substrates - Google Patents
Deposition of silicon germanium on silicon-on-insulator structures and bulk substrates Download PDFInfo
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Abstract
Description
発明の分野
本発明は、一般に、集積回路製造における、シリコンゲルマニウム−オン−インシュレーター(silicon−germanium−on−insulator)(「SGOI」)技術を含む、歪み緩和(strain relaxed)シリコンゲルマニウム上のストレインドシリコン(strained silicon)に関する。
FIELD OF THE INVENTION The present invention generally relates to a strain relaxed on strain relaxed silicon germanium, including silicon-germanium-on-insulator (“SGOI”) technology in integrated circuit manufacturing. It relates to silicon (strained silicon).
発明の背景技術
デバイスパフォーマンスを改善するために、従来の「バルク」シリコンウエハを、いわゆるシリコン−オン−インシュレーター(「SOI」)ウエハに置換することが開発される傾向にある。SOI技術の利点は、トランジスタが作られるシリコンがウエハの残りの部分と電気的接触しておらず、その結果、トランジスタ間でのクロストーク(cross−talk)がウエハバルクを通して生じないことである。これらのトランジスタは、互いからより有効に電気的に絶縁される。
Background of the Invention In order to improve device performance, there is a trend towards replacing conventional “bulk” silicon wafers with so-called silicon-on-insulator (“SOI”) wafers. The advantage of SOI technology is that the silicon from which the transistors are made is not in electrical contact with the rest of the wafer so that cross-talk between the transistors does not occur through the wafer bulk. These transistors are more effectively electrically isolated from each other.
SOI技術は、代表的には、アクティブ半導体層とウエハとの間の、ウエハの全体を横切った、または少なくともアクティブデバイスが半導体層中で形成されるエリアにおいて、薄い(例えば、約100nm)絶縁層を使用する。酸化ケイ素、窒化ケイ素またはこれら2つのコンビネーションは、絶縁層として典型的に使用される。これらの材料はアモルファスであり、優れた電気的な特性を有し、そして窒化ケイ素及び/または酸化ケイ素を集積するための技術は非常によく開発されている。 SOI technology typically involves a thin (eg, about 100 nm) insulating layer between the active semiconductor layer and the wafer, across the entire wafer, or at least in areas where active devices are formed in the semiconductor layer. Is used. Silicon oxide, silicon nitride or a combination of the two are typically used as the insulating layer. These materials are amorphous, have excellent electrical properties, and techniques for integrating silicon nitride and / or silicon oxide are very well developed.
SOI構造を形成する2つの従来技術が開発されている。SIMOXとして知られている1つの技術は、シリコンウエハのような半導体構造を用いて開始し、そして酸素原子の高エネルギー注入を使用して、シリコンウエハ表面下に、約100nmより大きな酸化被膜を形成する。次いで、高温のアニーリングによって、内部に(buried)酸化ケイ素が形成され、そして同時に注入により作製された表面のシリコン中の結晶欠陥を修復する。表面のシリコンは、半導体材料のままであり、そしてその結晶構造はアニーリングプロセスによって回復する。しかし、これらのステップは、幾分高価であり、そして絶縁層及びその上のアクティブシリコンの品質は幾分か悪い。 Two prior art techniques for forming SOI structures have been developed. One technique, known as SIMOX, starts with a semiconductor structure such as a silicon wafer, and uses high energy implantation of oxygen atoms to form an oxide film larger than about 100 nm below the silicon wafer surface. To do. High temperature annealing then forms a buried silicon oxide and simultaneously repairs the crystal defects in the surface silicon produced by implantation. The surface silicon remains a semiconductor material and its crystal structure is recovered by the annealing process. However, these steps are somewhat expensive and the quality of the insulating layer and the active silicon on it is somewhat poor.
SOI構造を形成するための別の方法は、酸化したシリコンウエハ上に犠牲シリコンウエハ(sacrificial silicon wafer)をボンディングすることに基づく。研削または他のシンニングプロセス(thinning process)によって、犠牲シリコンウエハが薄くされて、他方の基板の酸化物上の、非常に薄いアクティブ半導体層となる。しかし、アクティブ半導体層の最終的に所望される厚さの均一性が5nm±0.1nmであるので、シンニングプロセスは、SOI構造における高品質を達成するのに決定的に重要である。さらに、ボンディング及びシンニングのプロセスは複雑であり、やや高価である。 Another method for forming an SOI structure is based on bonding a sacrificial silicon wafer onto an oxidized silicon wafer. By grinding or other thinning process, the sacrificial silicon wafer is thinned into a very thin active semiconductor layer on the oxide of the other substrate. However, since the final desired thickness uniformity of the active semiconductor layer is 5 nm ± 0.1 nm, the thinning process is critical to achieving high quality in the SOI structure. Furthermore, the bonding and thinning processes are complex and somewhat expensive.
ストレインドシリコンは、キャリア移動度、ひいてはトランジスタの演算速度を増加させるために利用される。代表的には、シリコンゲルマニウム(SiGe)の薄層が基板上に形成され、そしてシリコンの非常に薄い層がSiGe上に堆積される。シリコンはゲルマニウムより小さな格子定数を有し、そしてシリコン層が緩和SiGe上で成長する場合、ケイ素原子は、下地層においてより広く原子間隔を置いて整列する傾向がある。その結果、最上部のシリコン層は伸ばされるか、または歪んで、電気的キャリアがより少ない抵抗で流れること可能にしている。 Strained silicon is used to increase the carrier mobility and thus the computational speed of the transistor. Typically, a thin layer of silicon germanium (SiGe) is formed on the substrate and a very thin layer of silicon is deposited on the SiGe. Silicon has a smaller lattice constant than germanium, and when the silicon layer is grown on relaxed SiGe, the silicon atoms tend to align more widely apart in the underlying layer. As a result, the top silicon layer is stretched or distorted to allow electrical carriers to flow with less resistance.
ストレインドシリコン及びSOIは相補的な技術であり、そしてSiGe−オン−インシュレーター(SGOI)基板を作り上げるためのいくつかの試みがなされている。 Strained silicon and SOI are complementary technologies and several attempts have been made to create SiGe-on-insulator (SGOI) substrates.
発明の要旨
発明の1つの局面に従って、歪み緩和SiGe−オン−インシュレーター構造上にストレインドシリコンを形成するための方法は、CVDによってSOI基板上にアモルファスSiGe層を形成すること、及びSiGe層の融解を引き起こす温度で基板をアニーリングする工程を含んでいる。SiGe層由来のGeは、アニーリング温度で、下地のSi層中に拡散し、酸化物上に緩和SiGe層をもたらす。
SUMMARY OF THE INVENTION In accordance with one aspect of the invention, a method for forming strained silicon on a strain relaxed SiGe-on-insulator structure includes forming an amorphous SiGe layer on an SOI substrate by CVD, and melting the SiGe layer. Annealing the substrate at a temperature that causes the. Ge from the SiGe layer diffuses into the underlying Si layer at the annealing temperature, resulting in a relaxed SiGe layer on the oxide.
本発明の別の局面に従って、基板上に歪み緩和SiGe層を形成するための方法は、前駆物質としてトリシランを用いるCVDによって、シリコン層上に、アモルファスSiGe層を堆積することを含む。固相エピタキシーは、シリコン層上にSiGe層を結晶化させるために実施される。アモルファスのSiGe層を堆積する前に、シリコン層は、幾分かの結晶シリコン領域を露出しながら、酸化物の1未満のモノレイヤーで覆われる。 In accordance with another aspect of the present invention, a method for forming a strain relaxation SiGe layer on a substrate includes depositing an amorphous SiGe layer on a silicon layer by CVD using trisilane as a precursor. Solid phase epitaxy is performed to crystallize the SiGe layer on the silicon layer. Prior to depositing the amorphous SiGe layer, the silicon layer is covered with less than one monolayer of oxide, exposing some crystalline silicon regions.
本発明のさらなる局面において、基板上のシリコン層上に歪み緩和SiGe層を形成する方法は、低温でのSiGeのヘテロエピタキシーを含む。好ましくは、ストレインドSiGe層は、トリシラン及びゲルマニウム前駆物質からのCVDによって堆積される。発泡剤(例えば、HまたはHe)がSi/SiGeの界面または界面下に注入され、そしてSiGe層がアニールされる。アニーリングの間、SiGe層は緩和する。ストレインドシリコン層は、引き続き、緩和したSiGe層上に堆積することができる。 In a further aspect of the present invention, a method of forming a strain relaxed SiGe layer on a silicon layer on a substrate includes SiGe heteroepitaxy at low temperatures. Preferably, the strained SiGe layer is deposited by CVD from trisilane and germanium precursors. A blowing agent (eg, H or He) is injected at or below the Si / SiGe interface and the SiGe layer is annealed. During annealing, the SiGe layer relaxes. A strained silicon layer can subsequently be deposited on the relaxed SiGe layer.
本発明のこれら及び他の局面は、以下の詳細な説明及び添付の図面(これらは本発明を例示し、そして限定しないことを意味する)から容易に明らかになる。 These and other aspects of the invention will be readily apparent from the following detailed description and the accompanying drawings, which are meant to illustrate and not limit the invention.
好ましい実施形態の詳細な説明
好ましいプロセス
本明細書中に用いられる場合、「単結晶」または、「エピタキシャル」は、主とする大きな結晶構造(その中に許容される数の欠陥を有していてもよい)を記述するために用いられる。当業者は、層の結晶度がアモルファスから多結晶、そして単結晶へと連続的に落ちることを理解している;当業者は、低密度の欠陥が存在していても、結晶構造が単結晶またはエピタキシャルと考えられ得る場合を容易に決定することができる。
Detailed Description of the Preferred Embodiment
Preferred Process As used herein, “single crystal” or “epitaxial” is used to describe a predominantly large crystal structure that may have an acceptable number of defects therein. Used for. The person skilled in the art understands that the crystallinity of the layer falls continuously from amorphous to polycrystalline and single crystal; the person skilled in the art knows that the crystal structure is single crystal even in the presence of low density defects. Or it can be easily determined when it can be considered epitaxial.
用語「アモルファス」は、例えば、本明細書中に記載される固相エピタキシー(SPE)または融解プロセスによって、容易に再分配され得る小粒多結晶構造を包含する。 The term “amorphous” encompasses small grain polycrystalline structures that can be readily redistributed, for example, by solid phase epitaxy (SPE) or melting processes described herein.
エピタキシーとは、堆積層が下地層の結晶構造の延長としての役割を果たす堆積を示す。ヘテロエピタキシーは、下地層及び上層の堆積層が異なる材料のものである一種のエピタキシーである。 Epitaxy refers to deposition in which the deposited layer serves as an extension of the crystal structure of the underlying layer. Heteroepitaxy is a type of epitaxy in which the underlying layer and the upper deposited layer are of different materials.
ヘテロエピタキシー堆積技術は、当該分野において周知であり、実際、下地層と上層との間の格子の不整合によって結晶の歪みを形成することにおいて有利であると考えられている。典型的には、そのようなヘテロエピタキシャル層は、2つの層の格子定数が正確に整合しないように、単結晶シリコン構造上にシリコンゲルマニウムをエピタキシャリーに堆積することにより形成される。この歪みは、半導体構造内の電気的キャリア移動度を増加させ、それによりトランジスタの性能を増強するので、有利であると考えられている。SiGe障壁に基づく相補型金属酸化膜半導体電界効果トランジスタ(CMOS)について、価電子帯と伝導帯とのバンド不連続性が必要である。伸長方向に(tensily)歪んだSi及び圧縮方向に歪んだSiGeは、互い違いの(staggered)バンドオフセット(band offset)(タイプII ヘテロインターフェース)をもたらすが、Si上のストレインドSiGeに関する伝導帯オフセットは無視できる。主要な挑戦の1つは、滑らかな表面形態及びより少ない欠陥を有する緩和SiGe構造の利用可能性である。 Heteroepitaxy deposition techniques are well known in the art and are indeed believed to be advantageous in forming crystal distortions due to lattice mismatch between the underlayer and the top layer. Typically, such heteroepitaxial layers are formed by epitaxially depositing silicon germanium on a single crystal silicon structure such that the lattice constants of the two layers do not match exactly. This distortion is considered advantageous because it increases the electrical carrier mobility in the semiconductor structure, thereby enhancing the performance of the transistor. For complementary metal oxide semiconductor field effect transistors (CMOS) based on SiGe barriers, a band discontinuity between the valence band and the conduction band is required. Tensilely strained Si and compressively strained SiGe result in a staggered band offset (type II heterointerface), while the conduction band offset for strained SiGe on Si is Can be ignored. One of the major challenges is the availability of relaxed SiGe structures with smooth surface morphology and fewer defects.
歪み緩和SiGeを形成するための融解凝固プロセス(図9)
完全な歪み緩和SiGe層は、融解凝固プロセスを使用することによりSOI基板上に形成され得る。(その開示が本明細書中に参考として援用される、Sugiiら、J.Vac.Sci.Technol.B20(5):1891−1896(2002);Kutsukakeら、Jpn.J.Appl.Phys.42:L232−L234(2003)を参照のこと) )。薄いSiGe及びシリコン層が従来のSOIウエハ上で成長し、最上部のシリコン層が酸化し、そして高温アニーリングが実施されて、SiGe層を部分的に融解する。凝固により歪み緩和SiGe層が製造される。この層は、SOI基板上の最上部のシリコン層中へのゲルマニウムの拡散の結果として、均一な組成を有する。従って、緩和SiGe層は、SOIウエハの酸化物の直接上に残留する。得られる層は、好ましくは、約1×105cm−2未満、より好ましくは約1×103cm−2未満、そしてなおより好ましくは約1000cm−2未満の欠陥密度を有する。不運にも、Kutsukake及びSugiiにより開示されるような分子線エピタキシー(MBE)も従来の前駆物質を使用するCVDも、この文脈におけるα−SiGeの商業的に満足な堆積をすることができない。
Melt solidification process to form strain relaxed SiGe (Figure 9)
A complete strain relaxation SiGe layer can be formed on the SOI substrate by using a melt solidification process. (Sugii et al., J. Vac. Sci. Technol. B20 (5): 1891-1896 (2002), the disclosure of which is incorporated herein by reference; Kutsukake et al., Jpn. J. Appl. Phys. : See L232-L234 (2003)))). Thin SiGe and silicon layers are grown on a conventional SOI wafer, the top silicon layer is oxidized, and high temperature annealing is performed to partially melt the SiGe layer. A strain relaxation SiGe layer is produced by solidification. This layer has a uniform composition as a result of the diffusion of germanium into the top silicon layer on the SOI substrate. Thus, the relaxed SiGe layer remains directly on the oxide of the SOI wafer. The resulting layer preferably has a defect density of less than about 1 × 10 5 cm −2 , more preferably less than about 1 × 10 3 cm −2 , and even more preferably less than about 1000 cm −2 . Unfortunately, neither molecular beam epitaxy (MBE) as disclosed by Kutsukake and Sugii nor CVD using conventional precursors can produce commercially satisfactory deposition of α-SiGe in this context.
ここで、図1−5を参照して、好ましい実施形態に従う一般的方法が例示される。最初に、アモルファスまたは小粒状の多結晶SiGe層200が、シリコン−オン−インシュレーター(SOI)基板100(図1)上に堆積される。SOI基板は、例えば、SOITEC(Bernin,France)から市販されている。アモルファスまたは小粒状多結晶SiGe層を堆積することによって、下地のシリコン層における欠陥の形成が回避される。
Referring now to FIGS. 1-5, a general method according to a preferred embodiment is illustrated. Initially, an amorphous or small granular
アモルファスまたは小粒状の多結晶のSiGe層200の堆積は、例えば、ASM Americaから入手可能なEpsilonTM CVDリアクタのようなリアクタ中で化学気相成長法(CVD)によって実施される。好ましくは、堆積は、約350℃〜約700℃、より好ましくは約400℃〜約600℃の温度で、そして約1Torr〜ほぼ大気圧、より好ましくは50Torrから760Torr、最も好ましくは760Torrの圧力で、トリシラン(Si3H8)及びGeH4(または他のゲルマニウム前駆物質)を原料とする。好ましくは、主なキャリアは、約2〜約100slmのフローレートのH2である。堆積されたSiGe層のアモルファスまたは小粒状の多結晶の性質は、多数の異なる方法によって実現することができる。有利には、これらの条件(例えば、760Torr)の下での堆積は、500℃で40%[Ge]に関して300Å/分より高く、または475℃で50%[Ge]に関して200Å/分より高く、より好ましくは300Å/分より高い速度でα−SiGeを製造することができる。
The deposition of the amorphous or small granular
1つの実施形態において、堆積条件は、SiGeの堆積速度がSiGe層の再結晶の速度より速いように選択される。固相エピタキシー(SPE)またはランダムヌクリエーショングロース(random nucleation growth)(RNG)は、SiGe層を堆積させるとともに、その再結晶を導く。再結晶、または再成長の速度は、図6において示されるように、温度及びゲルマニウム濃度に依存する。再結晶の速度が堆積の速度より大きな場合、アモルファスまたは小粒状の多結晶の層は達成されない。従って、堆積速度より低いSPEまたはRNGの速度を維持し、そしてアモルファス層を達成するために、約50%のゲルマニウム濃度について、堆積温度は、好ましくは、約500℃以下、より好ましくは約475℃以下である。圧力及びキャリアガスフロー(例えば、H2フロー)は、所望の温度で堆積速度を最適化するように、CVDプロセスで調整される。 In one embodiment, the deposition conditions are selected such that the deposition rate of SiGe is faster than the rate of recrystallization of the SiGe layer. Solid phase epitaxy (SPE) or random nucleation growth (RNG) deposits a SiGe layer and leads to its recrystallization. The rate of recrystallization or regrowth depends on temperature and germanium concentration, as shown in FIG. If the recrystallization rate is greater than the deposition rate, an amorphous or small granular polycrystalline layer is not achieved. Thus, to maintain a SPE or RNG rate below the deposition rate and achieve an amorphous layer, for a germanium concentration of about 50%, the deposition temperature is preferably about 500 ° C. or less, more preferably about 475 ° C. It is as follows. Pressure and carrier gas flow (eg, H 2 flow) are adjusted in the CVD process to optimize the deposition rate at the desired temperature.
アモルファスまたは小粒状の多結晶SiGeは、酸化物で少なくとも部分的に覆われているシリコン層上へのCVDによるSiGeの堆積によっても実現され得る。
例えば、SiGe層は、SOI基板上の自然酸化膜(native oxide)に対して堆積され得る。好ましくは、酸化物は、シリコン表面上のモノレイヤーの少なくとも約4分の1、より好ましくはモノレイヤーの少なくとも約半分である。一方、完全なモノレイヤー未満(less than a full monolayer)が、好ましくは、幾分かの単結晶Siを露出させておくために、シリコン表面上に形成される。特定の実施形態において、モノレイヤーの半分の酸化物は、酸素環境中で、堆積温度で加熱することによって、SOI基板上に形成される。下記のようなSiGe層を融解するための高温処理の際、酸化物が還元され、凝固の際、均一なSiGe層の形成が導かれる。
Amorphous or small granular polycrystalline SiGe can also be realized by deposition of SiGe by CVD on a silicon layer that is at least partially covered with oxide.
For example, a SiGe layer can be deposited against a native oxide on an SOI substrate. Preferably, the oxide is at least about one quarter of the monolayer on the silicon surface, more preferably at least about half of the monolayer. On the other hand, less than a full monolayer is preferably formed on the silicon surface to keep some single crystal Si exposed. In certain embodiments, the monolayer half oxide is formed on an SOI substrate by heating at a deposition temperature in an oxygen environment. During the high-temperature treatment for melting the SiGe layer as described below, the oxide is reduced, and a uniform SiGe layer is formed upon solidification.
あるいは、より厚い化学酸化膜が、例えば、従来のSC1ソリューションによって、SiGe層の堆積前に、SOIウエハのSi表面上で形成され得る。この場合、堆積中のSiGe層の再成長は、下地の結晶シリコン層との接触の欠如に起因して可能ではない。その結果、SiGeの堆積のためのCVD条件は、再結晶及び結果としての欠陥を回避するためではなく、堆積速度及び前駆物質消費を最適化するために調整され得る。部分的な酸化被膜と同様に、SiGe層を融解するための高温処理が酸化物を還元し、均一な組成の歪み緩和SiGe層の形成を可能にする。 Alternatively, a thicker chemical oxide can be formed on the Si surface of the SOI wafer prior to the deposition of the SiGe layer, for example by a conventional SC1 solution. In this case, regrowth of the SiGe layer during deposition is not possible due to the lack of contact with the underlying crystalline silicon layer. As a result, the CVD conditions for SiGe deposition can be adjusted to optimize deposition rate and precursor consumption rather than to avoid recrystallization and resulting defects. Similar to the partial oxide film, the high temperature treatment to melt the SiGe layer reduces the oxide and allows the formation of a strain relaxed SiGe layer of uniform composition.
さらなる実施形態において、ホウ素、ヒ素、燐、SbまたはCのようなドーパントのほぼ1層までのモノレイヤーが、SiGe層の堆積前に基板表面上に形成される。この薄層は、SiGe層が堆積される際の、再成長を防ぐ。好ましくは、ドーパント前駆物質を含むガスの短いスパイクが、シリコン表面上にほぼ1層までのドーパントのモノレイヤーを製造するために、SiGe堆積プロセスの開始前に導入される。高温融解の際、この中間ドーパント層が拡散し、凝固の際の均一な歪み緩和SiGe層の形成をもたらす。 In further embodiments, up to approximately one monolayer of a dopant such as boron, arsenic, phosphorous, Sb or C is formed on the substrate surface prior to the deposition of the SiGe layer. This thin layer prevents regrowth as the SiGe layer is deposited. Preferably, a short spike of gas containing the dopant precursor is introduced before the start of the SiGe deposition process to produce up to approximately one dopant monolayer on the silicon surface. During high temperature melting, this intermediate dopant layer diffuses, resulting in the formation of a uniform strain relaxed SiGe layer upon solidification.
堆積されるSiGe層200の厚さは、高温融解から生じる歪み緩和SiGe層中のゲルマニウムの所望の濃度に基づいて決定される。特定の最終ゲルマニウム濃度を達成するのに必要な厚さは、堆積された層のゲルマニウム濃度及びSOIウエハ上の下地シリコン層(それはGe拡散によって消費される)の厚さに基づいて容易に計算することができる。
The thickness of the deposited
下地のシリコン層300は、好ましくは、約50Å〜約500Åの厚さを有する。それがより薄いSiGe層の使用及び/または堆積されたSiGe層におけるより低い初期ゲルマニウム濃度を可能にするので、より薄いシリコン層が好ましい。例えば、約20%のゲルマニウムを含む緩和SiGe層が、現在、工業において所望されている。従って、50Åのシリコン層がSOIウエハ上に存在する場合、40%のゲルマニウム濃度を有する50ÅのSiGe層が堆積され得る。融解及び凝固の際、ゲルマニウムは、下記のように、SiGe層からシリコン層へと拡散する。その結果、約20%のゲルマニウム濃度を有する100ÅのSiGe層になる。
The
好ましくは、堆積された層において得られるゲルマニウム濃度は、欠陥密度を最小限にするために約60%以下に、より好ましくは約50%以下である。図7において見出されるように、約60%ゲルマニウムの濃度より上では、欠陥密度は、SPEの間に有意に増加する。本明細書中に参考として援用される米国特許第6,346,732号を参照のこと。下記のように、高温融解が使用されるが、温度はSPEのための範囲を通して動き、従って、SPEの間の欠陥の形成が考えられる。 Preferably, the germanium concentration obtained in the deposited layer is about 60% or less, more preferably about 50% or less to minimize defect density. As can be seen in FIG. 7, above the concentration of about 60% germanium, the defect density increases significantly during SPE. See US Pat. No. 6,346,732, incorporated herein by reference. As described below, high temperature melting is used, but the temperature moves through the range for the SPE, and therefore the formation of defects during the SPE is considered.
SiGe層の堆積に続いて、キャップ層400が形成される(図2)。好ましくは、キャップ層は、SiGe層200上に直接形成される。キャップ層は、下記の、引き続く高温融解の間に、下地のSiGe層200からのGeの蒸発を防ぐ。平滑な界面を有するSiO2−キャップ層は、SiGe界面が粗くなるのを防ぐ。好ましくは、アモルファスシリコン層400は、SiGe層上に堆積される。アモルファスシリコン層400は、典型的には、CVDによって、好ましくはSiGe層200と同じ反応スペースにおいて堆積される。例えば、アモルファスSiGe堆積の後、GeH4のフローは止めることができ、そしてアモルファスシリコンの層は、同じ堆積温度でトリシランから成長することができる。
Following the deposition of the SiGe layer, a
堆積に続いて、アモルファスシリコン層は、好ましくは、酸化して、SiO2キャップ層600(図3)を形成する。好ましくは、酸化は、酸化環境に基板を曝露することにより実施される。当該分野において公知の任意の酸化剤、好ましくは、水または酸素を用いることができる。1つの実施形態において、乾燥酸素が用いられる。別の実施形態において、α−Si層400は湿式酸化される。酸化温度は、好ましくは、約800℃〜約900℃の間にある。1つの実施形態において、酸化は、高温アニールの間の酸化種(oxigenated species)の一時的添加による高温融解処理と組み合わせられる。酸素雰囲気は、好ましくは、高温融解のために取り除かれる。あるいは、酸化物(好ましくはSiO2)は、エキソサイチュ(ex−situ)で堆積され得る。1つの実施形態において、酸化物は、SiGe層のSPEを回避するのに十分低い温度で、エキソサイチュで堆積される。
Following deposition, the amorphous silicon layer is preferably oxidized to form a SiO 2 cap layer 600 (FIG. 3). Preferably, the oxidation is performed by exposing the substrate to an oxidizing environment. Any oxidant known in the art can be used, preferably water or oxygen. In one embodiment, dry oxygen is used. In another embodiment, the α-
次いで、基板は、好ましくは、例えば、N2またはAr雰囲気中のような非反応性環境中で高温融解に供される。高温で、SiGe層は、少なくとも部分的に融解する。融解プロセスの間、ゲルマニウムは、図4における矢印によって例示されるように、SiGe層200から下地のシリコン層300へと拡散する。図5において示されるように、凝固の際、均一の組成の歪み緩和SiGe層が製造される。有利には、垂直または貫通転位は、このプロセスによって最小限にされる。貫通転位は、好ましくは107cm−2未満、より好ましくは105cm−2未満、そして最も好ましくは1000cm−2である。
The substrate is then preferably subjected to high temperature melting in a non-reactive environment such as, for example, in an N 2 or Ar atmosphere. At high temperatures, the SiGe layer melts at least partially. During the melting process, germanium diffuses from the
高温アニーリングは、好ましくは、約950℃〜約1425℃の間で実施され、より好ましくはその温度は、約1000℃より高く約1425℃未満である。融解温度は、均一な歪み緩和SiGe層を形成するのに決定的に重要なパラメーターである。2つのSiO2層600、700の間のSiGe層500全体(Geが拡散したSi層を含む)が融解される場合、全ての結晶情報が失われ、そして得られる層は多結晶であり、歪み緩和エピタキシャル層ではない。上記のSugiiらを参照のこと。図8は、温度及びゲルマニウム濃度の関数としての固相及び液相曲線のグラフを示す。高温融解のための温度は、好ましくは、得られるSiGe層500における所定の最終ゲルマニウム濃度についての固相曲線のちょうど左側にある温度が選択される。例えば、堆積されたSiGe層200(図4)が60%のゲルマニウムを含み、得られるSiGe層500(図5)が40%のゲルマニウムを含む状況においては、初期SiGe層は、1150℃で融解する。しかし、得られるSiGe層は、その温度で固体である。従って、両方の層の完全な融解はなく、そして均一な歪み緩和エピタキシャルSiGe層500の形成を可能にするのに十分な結晶構造が維持される。しかし、1200℃の温度(40%Ge濃度について固相線のちょうど右端)が用いられる場合、最初のSiGe層200及び得られるSiGe層500の両方が融解する。結晶構造は残らず、そして結晶化は生じない。
High temperature annealing is preferably performed between about 950 ° C. and about 1425 ° C., more preferably the temperature is greater than about 1000 ° C. and less than about 1425 ° C. The melting temperature is a critical parameter for forming a uniform strain relaxation SiGe layer. When the
高温は、好ましくは、下地のシリコン層300の全体にわたってゲルマニウムが拡散するのに十分な長さの時間の間、維持され、均一なSiGe層500が生じる。従って、高温融解に適する時間は、下地のSi層の厚さ、堆積されたSiGe層の厚さ、堆積されたSiGe層のゲルマニウム濃度及び選択された温度でのシリコン中のゲルマニウムの拡散係数に基づいて決定することができる(Sugiiらを参照のこと)。好ましくは、融解温度は、最終[Ge]含有量に依存して、約1050℃−1300℃の融解温度で、1分〜12時間、より好ましくは1〜2時間維持される。従って、冷却することにより凝固させるよりも、得られるシリコンゲルマニウム層濃度が、選択されたアニール温度での固相曲線より下に下がるまでゲルマニウムの拡散をもたらすように、単一の温度が選択される。
The high temperature is preferably maintained for a length of time sufficient for germanium to diffuse throughout the
凝固に続いて、基板は、特定の用途のために所望されるようなさらなる処理に供され得る。典型的には、SiO2キャップ層400は、ケミカルエッチにより除去される。次いで、ストレインドシリコン層が、歪み緩和SiGe層上に、ヘテロエピタキシャリーに堆積される。 Following solidification, the substrate can be subjected to further processing as desired for a particular application. Typically, the SiO 2 cap layer 400 is removed by chemical etching. A strained silicon layer is then deposited heteroepitaxially on the strain relaxed SiGe layer.
低い欠陥密度を有する歪み緩和SiGeを形成するためのSPEプロセス(図10)
発明の別の局面において、歪み緩和SiGe層は、固相エピタキシーによって形成される。この実施形態において、エピタキシャル成長はSPEプロセスの間にSiGe/Si界面で分断(disrupt)される。好ましくは、エピタキシャル成長は、SiGe/Si界面に結晶構造が介在することにより分断される。この分断は、例えば、Si層自体の欠陥によって、またはSi層上に形成または堆積された物質によって引き起こされ得るが、これらに限定されない。
SPE process for forming strain relaxed SiGe with low defect density (FIG. 10)
In another aspect of the invention, the strain relaxation SiGe layer is formed by solid phase epitaxy. In this embodiment, the epitaxial growth is disrupted at the SiGe / Si interface during the SPE process. Preferably, the epitaxial growth is interrupted by the presence of a crystal structure at the SiGe / Si interface. This disruption can be caused by, for example, but not limited to, defects in the Si layer itself, or by materials formed or deposited on the Si layer.
SPEが分断されるので、基板とエピタキシャル成長層との間の歪みが緩和される。その結果、融解プロセスに関して上記されるように、歪み緩和SiGe層が製造され、そして貫通欠陥形成が最小限にされる。 Since SPE is divided, strain between the substrate and the epitaxial growth layer is relaxed. As a result, as described above with respect to the melting process, a strain relaxed SiGe layer is produced and through defect formation is minimized.
SiGeは、好ましくは、基板上に、アモルファス状または小粒多結晶形態で堆積される。この基板は、例えば、ブランケットシリコンウエハまたはSOIウエハであり得る。 SiGe is preferably deposited on the substrate in an amorphous or small polycrystalline form. This substrate can be, for example, a blanket silicon wafer or an SOI wafer.
SiGeの堆積は、好ましくは、CVDによる。好ましくは、SiGeは、トリシラン及びGeH4、ジゲルマンまたは他のGe前駆物質から堆積される。高温融解プロセスについて上記されるように、アモルファスSiGeを堆積するために、堆積温度は、好ましくは、再成長速度が堆積速度より遅く、しかし商業上許容される堆積速度(好ましくは、100Å/分より高く、より好ましくは約200Å/分〜600Å/分の間)であるのに充分に低い。温度、圧力及びH2キャリアのフローは、所定の温度及びゲルマニウム濃度で堆積速度を最適化するように調整される。1つの実施形態において、SiGeは、475℃の温度で、トリシラン及びGeH4から、CVDによって堆積される。別の実施形態において、堆積温度は500℃である。好ましくは、堆積温度は、約400C〜約600℃の間である。 The deposition of SiGe is preferably by CVD. Preferably, SiGe is deposited from trisilane and GeH 4 , digermane or other Ge precursor. As described above for the high temperature melting process, to deposit amorphous SiGe, the deposition temperature is preferably set so that the regrowth rate is slower than the deposition rate, but a commercially acceptable deposition rate (preferably less than 100 Å / min. High, more preferably low enough to be between about 200 liters / minute and 600 liters / minute). Temperature, pressure and H 2 carrier flow are adjusted to optimize the deposition rate at a given temperature and germanium concentration. In one embodiment, SiGe is deposited by CVD from trisilane and GeH 4 at a temperature of 475 ° C. In another embodiment, the deposition temperature is 500 ° C. Preferably, the deposition temperature is between about 400C and about 600 ° C.
基板上に堆積されるSiGe層の厚さは、歪み緩和SiGe層の中のゲルマニウムの所望の濃度に基づいて決定される。このプロセスはGe拡散なしで実施され得るので、上記の高温融解の場合と異なり、SiGe層の中のゲルマニウムの濃度が処理中に変化する必要はない。従って、層の中の初期ゲルマニウム濃度と最終ゲルマニウム濃度は、好ましくは同一である。 The thickness of the SiGe layer deposited on the substrate is determined based on the desired concentration of germanium in the strain relaxed SiGe layer. Since this process can be performed without Ge diffusion, unlike the high temperature melting case described above, the concentration of germanium in the SiGe layer need not change during processing. Therefore, the initial germanium concentration and the final germanium concentration in the layer are preferably the same.
しかし、堆積された層におけるゲルマニウム濃度は、欠陥密度を最小限にするために、好ましくは約60%以下、より好ましくは約50%以下である。図7に見出されるように、約60%ゲルマニウム濃度より上では、欠陥密度は、SPEの間に有意に増加する。本明細書中に参考として援用される、米国特許第6,346,732号を参照のこと。従って、堆積されるSiGe層は、好ましくは、約0%〜約60%の間、より好ましくは、約20%〜約50%の間のゲルマニウム濃度を有している。 However, the germanium concentration in the deposited layer is preferably about 60% or less, more preferably about 50% or less in order to minimize defect density. As can be seen in FIG. 7, above about 60% germanium concentration, the defect density increases significantly during SPE. See US Pat. No. 6,346,732, incorporated herein by reference. Accordingly, the deposited SiGe layer preferably has a germanium concentration between about 0% to about 60%, more preferably between about 20% to about 50%.
エピタキシャル成長は、基板表面上の1未満の酸化物モノレイヤーの存在によって分断される。1つの実施形態において、酸化物は自然酸化膜である。別の実施形態において、酸化物は、基板上に故意に成長させられる。好ましくは、酸化物は、完全なモノレイヤー未満、より好ましくはモノレイヤーの4分の3未満、なおより好ましくはモノレイヤーの半分未満(3.5×1014cm−2)である。特定の実施形態において、酸化物の半分のモノレイヤーが、堆積温度での酸素環境における加熱によって、基板上に形成される。 Epitaxial growth is disrupted by the presence of less than one oxide monolayer on the substrate surface. In one embodiment, the oxide is a native oxide film. In another embodiment, the oxide is intentionally grown on the substrate. Preferably, the oxide is less than a complete monolayer, more preferably less than three quarters of the monolayer, and even more preferably less than half of the monolayer (3.5 × 10 14 cm −2 ). In certain embodiments, a half monolayer of oxide is formed on the substrate by heating in an oxygen environment at the deposition temperature.
1つの実施形態において、1層より厚いモノレイヤーの酸化物層が形成される。次いで、酸化物は、エッチングされるかそうでなければ還元されて、少なくとも幾分かの単結晶Siを露出する。例えば、より厚い化学酸化膜が、基板表面上に形成され得る。次いで、この化学酸化膜が、好ましくは、モノレイヤー未満、より好ましくはモノレイヤーの約半分未満までエッチングされる。エッチプロセスは、アモルファスSiGeの堆積の前に実施される。 In one embodiment, a monolayer oxide layer thicker than one layer is formed. The oxide is then etched or otherwise reduced to expose at least some single crystal Si. For example, a thicker chemical oxide film can be formed on the substrate surface. The chemical oxide is then preferably etched to less than a monolayer, more preferably less than about half of the monolayer. An etch process is performed prior to the deposition of amorphous SiGe.
SiGe層の堆積後、固相エピタキシーが実施される。これらの方法は当該分野において周知である。例えば、米国特許第6,346,732号を参照のこと。好ましくは、基板は、約30分間、約500℃〜約900℃の間の温度まで加熱される。 After deposition of the SiGe layer, solid phase epitaxy is performed. These methods are well known in the art. See, for example, US Pat. No. 6,346,732. Preferably, the substrate is heated to a temperature between about 500 ° C. and about 900 ° C. for about 30 minutes.
1つの実施形態において、自然酸化膜のような酸化物の薄層が、SPEプロセスの前にSiGe層上に形成される。周囲(または任意の酸化雰囲気)にSiGe層を曝露して、SPEプロセスの前に薄い(自然)酸化膜を形成することは、SPEの間の表面の平滑さをさらに改善するのを助け得る。 In one embodiment, a thin layer of oxide, such as a native oxide, is formed on the SiGe layer prior to the SPE process. Exposing the SiGe layer to the surroundings (or any oxidizing atmosphere) to form a thin (native) oxide film prior to the SPE process can help further improve the surface smoothness during the SPE.
SPE後に、シリコンの層が、SiGe上に、ヘテロエピタキシャリーに堆積され得る。SiGe層の緩んだ性質は、エピタキシャルシリコン層の中に歪みを生む。酸化物がSPEの前にSiGe層上に堆積された場合、酸化物は、好ましくは、シリコン層の堆積の前に除去される。 After SPE, a layer of silicon can be deposited heteroepitaxially on SiGe. The relaxed nature of the SiGe layer creates strain in the epitaxial silicon layer. If oxide is deposited on the SiGe layer prior to SPE, the oxide is preferably removed prior to deposition of the silicon layer.
バルク基板上にSPEによって製造され、最上部にストレインドSi層を有する、歪み緩和SiGeを含む層スタックは、層トランスファー技術によって酸化ハンドルウエハの最上部にトランスファーされ、残留SiGeの選択的な除去によってストレインドSi(のみ)オンインシュレーター(sSOI)を形成する。任意の層トランスファー技術(例えば、Smart−Cut/UnibondTM技術(SOITEC(Bernin,France)製)、Bond and Etch−back or Epitaxial−Layer transfer法(ELTRANTM;Canon NY,USA)またはNanocleaveTM layer transfer法(SiGen製(CA,USA)))が用いられ得る。 A layer stack comprising strain relaxed SiGe, fabricated by SPE on a bulk substrate and having a strained Si layer on the top, is transferred to the top of the oxidized handle wafer by layer transfer technology and selectively removed by residual SiGe. A strained Si (only) on insulator (sSOI) is formed. Any layer transfer technique (e.g., manufactured by Smart-Cut / Unibond TM technology (SOITEC (Bernin, France)) , Bond and Etch-back or Epitaxial-Layer transfer process (ELTRAN TM; Canon NY, USA ) or Nanocleave TM layer transfer Method (SiGen (CA, USA)) can be used.
歪み緩和SiGeを形成するためのヘテロエピタキシー、その後の注入及びアニール(図11)
本発明の別の局面において、歪み緩和SiGe層は、Si上のSiGeのヘテロエピタキシー、その後の発泡剤の注入及びSiGe層を緩和するための引き続くアニーリングによって形成される。歪み緩和の間の欠陥の形成は、下部Si層と上部SiGe層との間の結晶界面の分断によって防がれる。例えば、その開示が本明細書中に参考として援用される、Luysberg J.Applied Physics October 15th 2002;Herzogら、IEEE Electron Device Letters 23:485(2002);及びHuangeら、Appl.Phys.Lett 78:1267(2001)を参照のこと。
Heteroepitaxy to form strain relaxed SiGe, followed by implantation and annealing (FIG. 11)
In another aspect of the present invention, a strain-relaxed SiGe layer is formed by heteroepitaxy of SiGe on Si, followed by implantation of a blowing agent and subsequent annealing to relax the SiGe layer. The formation of defects during strain relaxation is prevented by breakage of the crystal interface between the lower Si layer and the upper SiGe layer. See, for example, Luysberg J., the disclosure of which is incorporated herein by reference. Applied Physics October 15th 2002; Herzog et al., IEEE Electron Devices Letters 23: 485 (2002); and Huange et al., Appl. Phys. Lett 78: 1267 (2001).
本質的に上に記述されるように、SiGeは、好ましくは、シリコン前駆物質及びゲルマニウム前駆物質からCVDによってエピタキシャリーに堆積される。好ましくは、シリコン前駆物質はトリシランである。1つの実施形態において、ゲルマニウム前駆物質はジゲルマンである。堆積温度は、好ましくは約350℃〜約700℃、より好ましくは約400℃〜約600℃である。 As described essentially above, SiGe is preferably deposited epitaxially from a silicon precursor and a germanium precursor by CVD. Preferably, the silicon precursor is trisilane. In one embodiment, the germanium precursor is digermane. The deposition temperature is preferably about 350 ° C to about 700 ° C, more preferably about 400 ° C to about 600 ° C.
SiGe層は、好ましくは、層が堆積温度で緩和する臨界厚さ以下の厚さに堆積される。従って、堆積されたSiGe層は、歪んだままである。臨界厚さが温度に依存するので、堆積は、好ましくは、全体的な層の厚さを最大限にするために、低温で実施される。それがより高いアニーリング温度で緩和するので、より厚い層が好ましい。 The SiGe layer is preferably deposited to a thickness below the critical thickness at which the layer relaxes at the deposition temperature. Thus, the deposited SiGe layer remains distorted. Since the critical thickness is temperature dependent, the deposition is preferably carried out at a low temperature to maximize the overall layer thickness. A thicker layer is preferred because it relaxes at higher annealing temperatures.
1つの実施形態において、SiGe層は、約50〜約200nmの厚さ、より好ましくは約100〜約150nmの厚さまで堆積される。 In one embodiment, the SiGe layer is deposited to a thickness of about 50 to about 200 nm, more preferably about 100 to about 150 nm.
ストレインドSiGe層の堆積後、発泡剤(例えば、イオン)は、SiGe層の真下に、好ましくはSi/SiGe界面もしくはその下に注入される。より好ましくは、発泡剤は、Si/SiGe界面の下約50nm〜約100nmに注入される。1つの実施形態において、発泡剤はH+である。別の実施形態において、発泡剤はHe+である。 After deposition of the strained SiGe layer, a blowing agent (eg, ions) is implanted directly below the SiGe layer, preferably at or below the Si / SiGe interface. More preferably, the blowing agent is injected from about 50 nm to about 100 nm below the Si / SiGe interface. In one embodiment, the blowing agent is H + . In another embodiment, the blowing agent is He + .
発泡剤は、Si/SiGe界面で結晶構造を中断させるのに十分な量注入される。特定の実施形態において、約1×1016イオンcm−2〜約1×1017イオンcm−2が注入される。 The blowing agent is injected in an amount sufficient to disrupt the crystal structure at the Si / SiGe interface. In certain embodiments, about 1 × 10 16 ions cm −2 to about 1 × 10 17 ions cm −2 are implanted.
Si/SiGe界面での酸素の注入も企図される。特に、酸素の注入が、SOI基板上に充分に緩和されたSiGe層を形成するために用いられ得る。例えば、本明細書中に参考として援用される、Sugiyamaら、Thin Solid Films 369:199(2000)を参照のこと。 Oxygen implantation at the Si / SiGe interface is also contemplated. In particular, oxygen implantation may be used to form a fully relaxed SiGe layer on the SOI substrate. See, for example, Sugiyama et al., Thin Solid Films 369: 199 (2000), incorporated herein by reference.
引き続くSiGe層のアニーリングは、層の緩和を導く。好ましくは、アニーリングは、約400℃〜約1000℃の間、より好ましくは約700℃〜約850℃の間の温度で、実施される。アニーリングは、好ましくは、約1分〜約12時間、より好ましくは約1分〜約1時間、より好ましくは10分間実行される。アニーリング温度では、泡は、注入された発泡剤(例えばHまたはHe)から形成され、そしてパンチアウト転位ループを作り出す。この転位ループは、Si/SiGe界面まで移動するかそうでなければ広がり、不整合な転位を緩和する歪みを形成する。さらに、層が臨界厚さ未満に堆積されるので、それは、引き続き、アニールプロセスまで歪んだままである(この点において、点緩和は、注入により作り出された欠陥と適応している)。従って、広がった結晶欠陥(例えば、貫通転位)が回避される。好ましくは、107貫通転位未満が、SiGe層中に存在し、より好ましくは105未満、そしてなおより好ましくは103未満である。 Subsequent annealing of the SiGe layer leads to layer relaxation. Preferably, the annealing is performed at a temperature between about 400 ° C and about 1000 ° C, more preferably between about 700 ° C and about 850 ° C. Annealing is preferably performed for about 1 minute to about 12 hours, more preferably about 1 minute to about 1 hour, more preferably 10 minutes. At the annealing temperature, the foam is formed from the injected blowing agent (eg H or He) and creates a punch-out dislocation loop. This dislocation loop migrates to the Si / SiGe interface or otherwise widens, creating a strain that relaxes misfit dislocations. Furthermore, as the layer is deposited below the critical thickness, it continues to be distorted until the annealing process (in this regard, point relaxation is accommodated with defects created by implantation). Thus, extended crystal defects (eg threading dislocations) are avoided. Preferably, less than 10 7 threading dislocations are present in the SiGe layer, more preferably less than 10 5 , and even more preferably less than 10 3 .
Siキャップ層は、好ましくは、SiGe層上に堆積されて、ストレインドシリコン層を作り出す。1つの実施形態において、SiGeキャップ層は、アニーリングの後に堆積される。しかし、好ましくは、キャップ層は、アニーリングの前に堆積される。例えば、約10〜約15nm厚さのストレインドシリコンのキャップ層は、アニーリング前に、ストレインドSiGe層上に堆積され得る。 A Si cap layer is preferably deposited on the SiGe layer to create a strained silicon layer. In one embodiment, the SiGe cap layer is deposited after annealing. However, preferably the cap layer is deposited prior to annealing. For example, a strained silicon cap layer of about 10 to about 15 nm thickness can be deposited on the strained SiGe layer prior to annealing.
さらなる実施形態において、得られる層スタックは、ハンドルウエハに移送される。 In a further embodiment, the resulting layer stack is transferred to a handle wafer.
前述の本発明は、特定の好ましい実施形態を用いて記載されたが、その他の実施形態は、本明細書中の開示を考慮して当業者に明白となる。従って、本発明は、好ましい実施形態の引用によって限定されることは意図されず、もっぱら添付の特許請求の範囲を参照して定義されることが意図される。 Although the foregoing invention has been described using certain preferred embodiments, other embodiments will become apparent to those skilled in the art in view of the disclosure herein. Accordingly, the invention is not intended to be limited by reference to the preferred embodiments, but is intended to be defined solely with reference to the appended claims.
Claims (26)
該アモルファスSiGe層上にSiO2層を堆積すること;及び
該SiO2層を堆積した後、1000℃より高い温度で該アモルファスSiGe層を融解することにより、該第1のゲルマニウム濃度よりも低い第2のゲルマニウム濃度を有するSiGe部分を有するSiGe−オン−インシュレーター基板を形成すること;
を含む、
SiGe−オン−インシュレーター(SiGe−on insulator)基板を形成する方法。 Depositing an amorphous SiGe layer having a first germanium concentration on one or less monolayers of dopant on a silicon-on-insulator (SOI) substrate by chemical vapor deposition (CVD);
Depositing a SiO 2 layer on the amorphous SiGe layer; and, after depositing the SiO 2 layer, melting the amorphous SiGe layer at a temperature higher than 1000 ° C. to lower the first germanium concentration lower than the first germanium concentration. Forming a SiGe-on-insulator substrate having a SiGe portion having a germanium concentration of 2;
including,
A method of forming a SiGe-on insulator substrate.
該堆積されたSiGe層を歪み緩和単結晶構造へと変換すること;及び
該歪み緩和SiGe層上に第二Si層をヘテロエピタキシャリーに堆積して、ストレインド第二Si層を形成すること、
を含み、該歪み緩和SiGe層が107未満の貫通転位を有し、
前記ストレインドSiGe層の歪み緩和単結晶構造への変換が、該SiGe層を堆積する前であり且つ固相エピタキシーを実施する前に、1以下のモノレイヤーのドーパントを存在させることを含む、緩和SiGe層上にストレインドシリコン層を形成する方法。 Depositing a SiGe layer from trisilane and germanium precursor on the first Si layer by CVD, thereby forming an interface between the first Si layer and the SiGe layer;
Converting the deposited SiGe layer into a strain-relaxed single crystal structure; and depositing a second Si layer on the strain-relaxed SiGe layer heteroepitaxially to form a strained second Si layer;
The strain relaxed SiGe layer has threading dislocations of less than 10 7 ;
Relaxation wherein the conversion of the strained SiGe layer to a strain-relieved single crystal structure includes the presence of no more than one monolayer dopant prior to depositing the SiGe layer and prior to performing solid phase epitaxy. A method of forming a strained silicon layer on a SiGe layer.
該アモルファスSiGe層を融解することが、該SOI基板のシリコンの部分を融解することをさらに含む、請求項1に記載の方法。 The SOI substrate has a silicon portion covering an oxide portion;
The method of claim 1, wherein melting the amorphous SiGe layer further comprises melting a silicon portion of the SOI substrate.
該アモルファスSiGe層を融解することが、該SOI基板のシリコンの部分にゲルマニウムを拡散させることをさらに含む、請求項1に記載の方法。 The SOI substrate has a silicon portion covering an oxide portion;
The method of claim 1, wherein melting the amorphous SiGe layer further comprises diffusing germanium into a silicon portion of the SOI substrate.
該SiGe−オン−インシュレーター基板のSiGeの部分を、該酸化物の部分に接触させる、請求項1に記載の方法。 The SOI substrate has a silicon portion covering an oxide portion;
The method of claim 1, wherein a SiGe portion of the SiGe-on-insulator substrate is contacted with the oxide portion.
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Also Published As
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US20070042572A1 (en) | 2007-02-22 |
KR20060056331A (en) | 2006-05-24 |
US20050054175A1 (en) | 2005-03-10 |
JP5601595B2 (en) | 2014-10-08 |
WO2005010946A2 (en) | 2005-02-03 |
JP2007505477A (en) | 2007-03-08 |
WO2005010946A3 (en) | 2006-09-08 |
EP1647046A2 (en) | 2006-04-19 |
US7208354B2 (en) | 2007-04-24 |
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